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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5616926insertion1nstd207human GRCh38 chr2: 85,817,544-85,817,544 , GRCh37.p13 chr2: 86,044,667-86,044,667 LOC284950
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4728539copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,786,006-86,559,358 , GRCh38.p12 chr2: 85,558,883-86,332,235 ST3GAL5-AS1, TMEM150A, 25 more genes
    nsv4519695copy number variation1nstd166human GRCh37.p13 chr2: 85,888,999-87,236,000 , GRCh38.p12 chr2: 85,661,876-87,008,877 , RNF103, 33 more genes
    nsv4453381copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,948,835-86,438,539 , GRCh38.p12 chr2: 85,721,712-86,211,416 MIR6071, MRPL35, 12 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 REEP1, RBX1P1, 134 more genes
    nsv3968749insertion1nstd168human GRCh38 chr2: 85,822,633-85,847,499 , GRCh37.p13 chr2: 86,049,756-86,074,622 LOC284950, ST3GAL5
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 NAGK, NRXN1-DT, 595 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3899461copy number variation1nstd102humanPathogenic GRCh38 chr2: 85,014,686-88,826,619 , GRCh37 chr2: 85,241,809-89,126,132 , NCBI36 chr2: 85,095,320-88,907,247 CD8A, RNU6-1007P, 115 more genes
    nsv3897079copy number variation1nstd102humanPathogenic GRCh38 chr2: 77,025,216-90,282,666 , NCBI36 chr2: 77,105,850-90,982,989 , GRCh37 chr2: 77,252,342-91,619,262 IGKV2D-18, RPIA, 280 more genes
    nsv3886532copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975 RNU6-561P, VAMP5, 249 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
    nsv3882844copy number variation1nstd102humanUncertain significance GRCh37 chr2: 82,517,612-86,262,705 , GRCh38.p12 chr2: 82,290,488-86,035,582 TMEM150A, RNU1-38P, 69 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTND2P22, LOC112268410, 3724 more genes
    nsv3877742copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551 RNU6-561P, M1AP, 253 more genes
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